Medaglini D, Rush C M, Sestini P, Pozzi G
Dipartimento di Biologia Molecolare, Università di Siena, Italy.
Vaccine. 1997 Aug-Sep;15(12-13):1330-7. doi: 10.1016/s0264-410x(97)00026-1.
There is a need to develop vaccines to control the spread of sexually transmitted diseases (STDs). Novel immunization strategies that elicit a mucosal immune response in the genital tract, may show improved protection by preventing or at least limiting entry of the pathogenic micro-organism. However, it has proven difficult to obtain a local immune response in the vaginal mucosa. Our approach is based on the use of recombinant bacteria capable of colonizing mucosal surfaces as live vaccine vectors. The human commensal Streptococcus gordonii, engineered to express the E7 protein of human papillomavirus type 16, was used for intravaginal immunization of mice. A single inoculum of recombinant bacteria was sufficient to establish colonization of the murine vagina and therefore induce papillomavirus-specific vaginal IgA and serum IgG. Evidence that mucosal colonization with recombinant commensal bacteria can induce a local immune response in the female genital tract represents a significant step toward the development of new vaccines against STDs.
有必要研发疫苗来控制性传播疾病(STD)的传播。能在生殖道引发黏膜免疫反应的新型免疫策略,或许可通过预防或至少限制致病微生物的侵入来提供更好的保护。然而,事实证明在阴道黏膜中引发局部免疫反应颇具难度。我们的方法基于使用能够定殖于黏膜表面的重组细菌作为活疫苗载体。经改造以表达人乳头瘤病毒16型E7蛋白的人共生菌戈登链球菌,被用于对小鼠进行阴道内免疫。单次接种重组细菌就足以在小鼠阴道中定殖,从而诱导出乳头瘤病毒特异性的阴道IgA和血清IgG。重组共生菌在黏膜定殖可在女性生殖道诱导局部免疫反应,这一证据代表着朝着研发新型性传播疾病疫苗迈出了重要一步。